Allele Registry

Canonical Allele Identifier: PA2826636689

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000218606

RCV000486781

RCV000629928

RCV000805703

RCV003166251

RCV003468985

RCV004001679

ClinVar Variation:

229859

650537

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Thr622Ser	CA069606 NM_001281494.2:c.1864A>T CA346755462 NM_001281494.2:c.1865C>G